US2019192633A1PendingUtilityA1
Treatment of depression and ptsd
Est. expiryOct 18, 2032(~6.2 yrs left)· nominal 20-yr term from priority
A61K 9/08A61K 38/24A61K 9/0019A61P 25/00A61K 9/19
56
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Claims
Abstract
Depression and PTSD are treated by administration of hCG, or an hCG analog, or a prodrug or metabolite of hCG or an hCG analog, in an amount equivalent to a subcutaneous dose of 50-200 IU, preferably 120-170 IU, more preferably 140-160 IU, of hCG per day.
Claims
exact text as granted — not AI-modified1 - 18 . (canceled)
19 . A method of treating an anxiety disorder in a subject that has experienced a serious injury, comprising administering to the subject hCG at a subcutaneous dosage of 50 IU per day to 200 IU per day or a dosage equivalent to a subcutaneous dosage amount of 50 IU per day to 200 IU per day, wherein the method of treating includes treating at least one symptom of the anxiety disorder.
20 . The method of claim 19 , wherein the anxiety disorder is a disorder that includes a symptom of avoiding stimuli associated with the serious injury.
21 . The method of claim 19 , wherein the anxiety disorder is a disorder that includes a symptom of re-experiencing one or more events related to the serious injury.
22 . The method of claim 19 , wherein the anxiety disorder is post traumatic stress disorder.
23 . The method of claim 19 , wherein the method comprises activating the central nervous system LH/hCG receptor.
24 . The method of claim 19 , wherein the hCG is administered as a subcutaneous dosage of between 120 IU per day and 170 IU per day of hCG.
25 . The method of claim 19 , wherein the hCG is administered as a dosage equivalent to a subcutaneous dosage amount of between 120 IU per day and 170 IU per day of hCG.
26 . The method of claim 19 , wherein the hCG is administered as a subcutaneous dosage of between 140 IU per day and 160 IU per day of hCG.
27 . The method of claim 19 , wherein the hCG is administered as a dosage equivalent to a subcutaneous dosage amount of between 140 IU per day and 160 IU per day of hCG.
28 . The method of claim 19 , wherein the hCG is administered once per day.
29 . The method of claim 19 , wherein the hCG is administered once daily for at least 1 week.
30 . The method of claim 19 , wherein the hCG is administered once daily for at least 3 weeks.
31 . The method of claim 19 , wherein the hCG is administered once daily for at least 6 weeks.
32 . The method of claim 19 , wherein the hCG is administered chronically.
33 . The method of claim 19 , wherein the hCG is administered as a subcutaneous dosage that consists essentially of hCG.
34 . A method of activating the central nervous system LH/hCG receptor in a subject, comprising administering to the subject hCG at a subcutaneous dosage of 50 IU per day to 200 IU per day or a dosage equivalent to a subcutaneous dosage amount of 50 IU per day to 200 IU per day.
35 . The method of claim 34 , wherein the hCG is administered as a subcutaneous dosage of between 120 IU per day and 170 IU per day of hCG.
36 . The method of claim 34 , wherein the hCG is administered as a dosage equivalent to a subcutaneous dosage amount of between 120 IU per day and 170 IU per day of hCG.
37 . The method of claim 34 , wherein the hCG is administered as a subcutaneous dosage of between 140 IU per day and 160 IU per day of hCG.
38 . The method of claim 34 , wherein the hCG is administered as a dosage equivalent to a subcutaneous dosage amount of between 140 IU per day and 160 IU per day of hCG.Join the waitlist — get patent alerts
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